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Comparison Of DIR-MRI And DCE-MRI In Detection Of Prostate Cancer: A Pilot Study

Comparison Of Double Inversion Recovery Magnetic Resonance Imaging (Dir-Mri) And Dynamic Contrast Enhanced Magnetic Imaging (Dce-Mri) In Detection Of Prostate Cancer: A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02939456
Acronym
DIRMP
Enrollment
150
Registered
2016-10-20
Start date
2016-06-30
Completion date
2017-04-30
Last updated
2019-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer of the Prostate

Keywords

prostate, cancer, MRI

Brief summary

This is a pilot study taking place at University Hospitals of North Midlands NHS Trust. Patients referred for MRI for possible prostate cancer will be invited to take part in the study. Following consent, participants will have an additional MRI sequence performed during their routine MRI called Double Inversion Magnetic Resonance Imaging (DIR-MRI). Participants scan images and prostate biopsy histology report (if applicable) will be reviewed by the research team.

Detailed description

This is a pilot study taking place at University Hospitals of North Midlands NHS Trust. Patients referred for MRI for possible prostate cancer will be invited to take part in the study. Following consent, participants will have an additional MRI sequence performed during their routine MRI called Double Inversion Magnetic Resonance Imaging (DIR-MRI). Participants scan images and prostate biopsy histology report (if applicable) will be reviewed by the research team. The research team will look at the variability of LNR score amongst the two scan typed and the DCE-MRI and DIR-MRI images will be correlated with biopsy results to give an indication of the accuracy.

Interventions

OTHERMagnetic Resonance Imaging

Double Inversion Recovery Magnetic Resonance Imaging (DIR-MRI) and Dynamic Contrast Enhanced Magnetic Imaging (DCE-MRI)

Sponsors

University Hospitals of North Midlands NHS Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients referred for prostate MRI for possible prostate cancer * Safe to undergo an MRI scan * Able to give informed consent

Exclusion criteria

* MRI referrals where prostate cancer is not the question * Patients who are not safe to undergo an MRI scan * Patients who have undergone prostate biopsy in the previous 10 weeks * Patients unable to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Lesion to Normal tissue Ratio (LNR) recorded for DIR-MRI and DCE-MRI3 monthsIn order to inform a sample size calculation for a subsequent, fully powered equivalence trial Is DIR-MRI equivalent to DCE-MRI in detection of prostate cancer

Secondary

MeasureTime frameDescription
Correlation of biopsy and DIR-MRI and DCE-MRI findings3 monthsIn order to ascertain if addition of DIR-MRI could improve accuracy of cancer diagnosis

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026